ORPHA:716422
Rare disorder with non-progressive predominantly macular disorder as a major feature
Synonyms: Rare syndromic non-progressive predominantly macular disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder with non-progressive predominantly macular disorder as a major feature | Rare syndromic non-progressive predominantly macular disorder |
| fr | Maladie rare avec atteinte non-progressive prédominante de la macula comme manifestation majeure rare | Maladie rare avec atteinte non-progressive prédominante de la macula syndromique |
| de | Seltene Störung mit nicht-progredienter Makulopathie als Hauptmerkmal | |
| es | Trastorno raro con afectación predominantemente macular no progresiva como característica principal | Trastorno raro predominantemente macular no progresivo sindrómico |
| it | Malattia rara con predominante maculopatia non progressiva come caratteristica principale | Malattia rara sindromica non progressiva a predominanza maculare |
| nl | Zeldzame aandoening met niet-progressieve overwegend maculaire aandoening als een hoofdkenmerk | Zeldzame syndromale niet-progressieve overwegend maculaire aandoening · Zeldzame syndromale niet-progressieve aandoening van voornamelijk macula · Zeldzame syndromale niet-progressieve aandoening van voornamelijk gele vlek |
| pt | Rare disorder with non-progressive predominantly macular disorder as a major feature | |
| pl | Rzadkie postępujące zaburzenie z zajęciem głównie plamki jako dominującą cechą | = en |
| cs | Rare disorder with non-progressive predominantly macular disorder as a major feature | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:717327Rare genetic non-progressive predominantly macular disorder
rare genetic diseases - ORPHA:716413Rare non-progressive predominantly macular disorder
rare ophthalmic disorders
Children (1):
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/716422
- This record as JSON: /data/d/716422.json